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GINOM: A statistical framework for assessing interval overlap of multiple genomic features
A common problem in genomics is to test for associations between two or more genomic features, typically represented as intervals interspersed across the genome. Existing methodologies can test for significant pairwise associations between two genomic intervals; however, they cannot test for associa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491313/ https://www.ncbi.nlm.nih.gov/pubmed/28617797 http://dx.doi.org/10.1371/journal.pcbi.1005586 |
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author | Bryner, Darshan Criscione, Stephen Leith, Andrew Huynh, Quyen Huffer, Fred Neretti, Nicola |
author_facet | Bryner, Darshan Criscione, Stephen Leith, Andrew Huynh, Quyen Huffer, Fred Neretti, Nicola |
author_sort | Bryner, Darshan |
collection | PubMed |
description | A common problem in genomics is to test for associations between two or more genomic features, typically represented as intervals interspersed across the genome. Existing methodologies can test for significant pairwise associations between two genomic intervals; however, they cannot test for associations involving multiple sets of intervals. This limits our ability to uncover more complex, yet biologically important associations between multiple sets of genomic features. We introduce GINOM (Genomic INterval Overlap Model), a new method that enables testing of significant associations between multiple genomic features. We demonstrate GINOM’s ability to identify higher-order associations with both simulated and real data. In particular, we used GINOM to explore L1 retrotransposable element insertion bias in lung cancer and found a significant pairwise association between L1 insertions and heterochromatic marks. Unlike other methods, GINOM also detected an association between L1 insertions and gene bodies marked by a facultative heterochromatic mark, which could explain the observed bias for L1 insertions towards cancer-associated genes. |
format | Online Article Text |
id | pubmed-5491313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54913132017-07-18 GINOM: A statistical framework for assessing interval overlap of multiple genomic features Bryner, Darshan Criscione, Stephen Leith, Andrew Huynh, Quyen Huffer, Fred Neretti, Nicola PLoS Comput Biol Research Article A common problem in genomics is to test for associations between two or more genomic features, typically represented as intervals interspersed across the genome. Existing methodologies can test for significant pairwise associations between two genomic intervals; however, they cannot test for associations involving multiple sets of intervals. This limits our ability to uncover more complex, yet biologically important associations between multiple sets of genomic features. We introduce GINOM (Genomic INterval Overlap Model), a new method that enables testing of significant associations between multiple genomic features. We demonstrate GINOM’s ability to identify higher-order associations with both simulated and real data. In particular, we used GINOM to explore L1 retrotransposable element insertion bias in lung cancer and found a significant pairwise association between L1 insertions and heterochromatic marks. Unlike other methods, GINOM also detected an association between L1 insertions and gene bodies marked by a facultative heterochromatic mark, which could explain the observed bias for L1 insertions towards cancer-associated genes. Public Library of Science 2017-06-15 /pmc/articles/PMC5491313/ /pubmed/28617797 http://dx.doi.org/10.1371/journal.pcbi.1005586 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Bryner, Darshan Criscione, Stephen Leith, Andrew Huynh, Quyen Huffer, Fred Neretti, Nicola GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title | GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title_full | GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title_fullStr | GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title_full_unstemmed | GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title_short | GINOM: A statistical framework for assessing interval overlap of multiple genomic features |
title_sort | ginom: a statistical framework for assessing interval overlap of multiple genomic features |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491313/ https://www.ncbi.nlm.nih.gov/pubmed/28617797 http://dx.doi.org/10.1371/journal.pcbi.1005586 |
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